A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463058



Internal ID22520943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211482058..211483389hg38UCSC Ensembl
chr1:211655400..211656731hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg381332
hg191332
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829335
Supporting Variants
Samples
Known GenesRD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463058
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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